Affiliation:
1. Department of Molecular Chemistry and Materials Science Weizmann Institute of Science Rehovot 7610001 Israel
Abstract
AbstractPincer ligand complexes, which appeared nearly five decades ago, have provided a valuable platform for the study of fundamental chemical processes and the development of efficient catalysts for many chemical transformations. These complexes have usually contained transition metal atoms or ions, and their respective pincer ligands have often featured phosphine donor groups, which strongly coordinate to the metal center and allow its steric and electronic properties to be fine‐tuned. The increasing need to develop cost‐effective and sustainable catalytic processes has driven the search for main‐group metals as alternatives to commonly‐used transition metals. In this review, we show that despite the inherent mismatch between phosphines, which are soft Lewis bases, and main‐group metal ions, which are hard Lewis acids, a series of well‐defined phosphine‐based pincer complexes containing Li(I), Na(I), K(I), Mg(II), Ca(II), Zn(II) and Al(III) have been reported, which have proven to be active catalysts for industrially‐relevant transformations.
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1. Transition metal–carbon bonds. Part XLII. Complexes of nickel, palladium, platinum, rhodium and iridium with the tridentate ligand 2,6-bis[(di-t-butylphosphino)methyl]phenyl
2. Tuning the reactivity of metals held in a rigid ligand environment
3. Pincer ligands are customarily classified according to the identity of the atoms that are directly bonded to the metal center and their relative position within the ligand. For example the pincer ligand shown in Figure 1a is coordinated to each metal center through two P atoms from the side-arms and an intervening C atom and is therefore classified as a PCP-type ligand.
4. Pincer and Pincer-Type Complexes
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